# Corum:digest

(Difference between revisions)
 Revision as of 13:49, 19 June 2012 (view source)m ← Previous diff Revision as of 13:50, 19 June 2012 (view source)m Next diff → Line 2: Line 2: ==Overview== ==Overview== - Standard DNA digest protocol using [http://www.neb.com | NEB] restriction enzymes. + Standard DNA digest protocol using [http://www.neb.com NEB] restriction enzymes. ==Materials== ==Materials== Line 9: Line 9: * ~0.8V DNA * ~0.8V DNA - * 0.1V 10X digestion buffer (1, 2, 3, or 4; NEB) + * 0.1V 10X digestion buffer (1, 2, 3, or 4; [http://www.neb.com NEB]) * 0.1V 10mg/ml BSA * 0.1V 10mg/ml BSA * 1 μL restriction enzyme 1 * 1 μL restriction enzyme 1 Line 15: Line 15: ==Procedure== ==Procedure== - # Find appropriate enzymes(s), associated buffer, reaction temperature from [http://www.neb.com | NEB]. + # Find appropriate enzymes(s), associated buffer, reaction temperature from [http://www.neb.com NEB]. # Calculate the total volume of the reaction by taking the DNA volume + 1(2) μL for a single (double) digestion reaction. Divide this number by 0.8 to get the total reaction volume, V. # Calculate the total volume of the reaction by taking the DNA volume + 1(2) μL for a single (double) digestion reaction. Divide this number by 0.8 to get the total reaction volume, V. # Calculate the volume of 10mg/ml BSA and 10X digestion buffer, which are both 0.1V. # Calculate the volume of 10mg/ml BSA and 10X digestion buffer, which are both 0.1V. Line 30: Line 30: ==References== ==References== - '''Relevant papers and books''' + '''Relevant papers, books, and websites''' - #[http://www.neb.com | New England Biolabs] + #[http://www.neb.com New England Biolabs] ==Contact== ==Contact==

## Revision as of 13:50, 19 June 2012

• SC 14:47, 19 June 2012 (EDT):

## Overview

Standard DNA digest protocol using NEB restriction enzymes.

## Materials

For a DNA digestion of total volume V (in μL):

• ~0.8V DNA
• 0.1V 10X digestion buffer (1, 2, 3, or 4; NEB)
• 0.1V 10mg/ml BSA
• 1 μL restriction enzyme 1
• 1 μL restriction enzyme 2 (optional, for double digestion)

## Procedure

1. Find appropriate enzymes(s), associated buffer, reaction temperature from NEB.
2. Calculate the total volume of the reaction by taking the DNA volume + 1(2) μL for a single (double) digestion reaction. Divide this number by 0.8 to get the total reaction volume, V.
3. Calculate the volume of 10mg/ml BSA and 10X digestion buffer, which are both 0.1V.
4. Add the reaction components together in order listed above. Mix gently and spin.
5. Incubate at reaction temperature for 3 hr to overnight.

## Notes

Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!

1. List troubleshooting tips here.
2. You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
3. Anecdotal observations that might be of use to others can also be posted here.

## References

Relevant papers, books, and websites

1. New England Biolabs